Zhaohui S. Qin
Orcid: 0000-0002-1583-146XAffiliations:
- Emory University, Atlanta, GA, USA
According to our database1,
Zhaohui S. Qin
authored at least 43 papers
between 2002 and 2023.
Collaborative distances:
Collaborative distances:
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Online presence:
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on id.loc.gov
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on d-nb.info
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Bibliography
2023
Editorial: AI and data science in drug development and public health: Highlights from the MCBIOS 2022 conference.
Frontiers Big Data, January, 2023
2022
IEEE ACM Trans. Comput. Biol. Bioinform., 2022
<i>LRcell</i>: detecting the source of differential expression at the sub-cell-type level from bulk RNA-seq data.
Briefings Bioinform., 2022
Disease category-specific annotation of variants using an ensemble learning framework.
Briefings Bioinform., 2022
2021
A wonderful time - exciting progress made in the past 20 years in genetics powered by the Human Genome Project.
Quant. Biol., December, 2021
Systematic Exploration in Tissue-Pathway Associations of Complex Traits Using Comprehensive eQTLs Catalog.
Frontiers Big Data, 2021
2020
Inferring Spatial Organization of Individual Topologically Associated Domains via Piecewise Helical Model.
IEEE ACM Trans. Comput. Biol. Bioinform., 2020
Proceedings of the 2019 MidSouth Computational Biology and Bioinformatics Society (MCBIOS) Conference.
BMC Bioinform., 2020
Application of topic models to a compendium of ChIP-Seq datasets uncovers recurrent transcriptional regulatory modules.
Bioinform., 2020
Bioinform., 2020
Briefings Bioinform., 2020
2019
RT States: systematic annotation of the human genome using cell type-specific replication timing programs.
Bioinform., 2019
2018
Probabilistic and machine learning-based retrieval approaches for biomedical dataset retrieval.
Database J. Biol. Databases Curation, 2018
2017
Quant. Biol., 2017
Nucleic Acids Res., 2017
Proceedings of the Data Management and Analytics for Medicine and Healthcare, 2017
2016
A hidden Markov random field-based Bayesian method for the detection of long-range chromosomal interactions in Hi-C data.
Bioinform., 2016
Bayesian inference with historical data-based informative priors improves detection of differentially expressed genes.
Bioinform., 2016
traseR: an R package for performing trait-associated SNP enrichment analysis in genomic intervals.
Bioinform., 2016
Proceedings of the Joint International Conference on Biological Ontology and BioCreative, 2016
2015
One Size Doesn't Fit All - RefEditor: Building Personalized Diploid Reference Genome to Improve Read Mapping and Genotype Calling in Next Generation Sequencing Studies.
PLoS Comput. Biol., 2015
A novel statistical method for quantitative comparison of multiple ChIP-seq datasets.
Bioinform., 2015
2013
Understanding spatial organizations of chromosomes via statistical analysis of Hi-C data.
Quant. Biol., 2013
A genome-wide MeSH-based literature mining system predicts implicit gene-to-gene relationships and networks.
BMC Syst. Biol., 2013
Sparsely correlated hidden Markov models with application to genome-wide location studies.
Bioinform., 2013
2012
Using Poisson mixed-effects model to quantify transcript-level gene expression in RNA-Seq.
Bioinform., 2012
Read-mapping using personalized diploid reference genome for RNA sequencing data reduced bias for detecting allele-specific expression.
Proceedings of the 2012 IEEE International Conference on Bioinformatics and Biomedicine Workshops, 2012
2010
A Double-Layered Mixture Model for the Joint Analysis of DNA Copy Number and Gene Expression Data.
J. Comput. Biol., 2010
BMC Bioinform., 2010
2009
Hierarchical hidden Markov model with application to joint analysis of ChIP-chip and ChIP-seq data.
Bioinform., 2009
2008
Data Analysis and Graphics Using R: An Example-Based Approach, Second Edition.: John Maindonald and John Braun.
Briefings Bioinform., 2008
2007
CRCView: a web server for analyzing and visualizing microarray gene expression data using model-based clustering.
Bioinform., 2007
2006
An efficient comprehensive search algorithm for tagSNP selection using linkage disequilibrium criteria.
Bioinform., 2006
Clustering microarray gene expression data using weighted Chinese restaurant process.
Bioinform., 2006
TagSNP Selection Based on Pairwise LD Criteria and Power Analysis in Association Studies.
Proceedings of the Biocomputing 2006, 2006
2005
High Throughput Screening of Co-Expressed Gene Pairs with Controlled False Discovery Rate (FDR) and Minimum Acceptable Strength (MAS).
J. Comput. Biol., 2005
BMC Bioinform., 2005
HapBlock: haplotype block partitioning and tag SNP selection software using a set of dynamic programming algorithms.
Bioinform., 2005
2003
Proceedings of the 2nd IEEE Computer Society Bioinformatics Conference, 2003
2002
Dynamic Programming Algorithms for Haplotype Block Partitioning and Tag SNP Selection Using Haplotype Data or Genotype Data.
Proceedings of the Computational Methods for SNPs and Haplotype Inference, 2002
Proceedings of the Computational Methods for SNPs and Haplotype Inference, 2002